A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552865



Internal ID15993588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:612843..626730hg38UCSC Ensembl
Innerchr11:612843..626730hg19UCSC Ensembl
Innerchr11:602843..616730hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813888
hg1913888
hg1813888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763560
Samples
Known GenesCDHR5, IRF7, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552865
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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